5 results on '"Hübers, Annemarie"'
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2. Serum microRNAs in sporadic amyotrophic lateral sclerosis
3. Polymerase chain reaction and Southern blot-based analysis of the C9orf72 hexanucleotide repeat in different motor neuron diseases
4. A novel phosphorylation site mutation in profilin 1 revealed in a large screen of US, Nordic, and German amyotrophic lateral sclerosis/frontotemporal dementia cohorts
5. De novo FUS mutations are the most frequent genetic cause in early-onset German ALS patients
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